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P9129

5-Pregnen-3β-ol-20-one

≥98%

Synonym(s):

3β-Hydroxy-5-pregnen-20-one, Pregnenolone

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Size/SKUAvailabilityPrice
1 g
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1 130,00 CZK
100 g
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12 300,00 CZK

About This Item

Empirical Formula (Hill Notation):
C21H32O2
CAS Number:
Molecular Weight:
316.48
UNSPSC Code:
12352211
NACRES:
NA.77
PubChem Substance ID:
EC Number:
205-647-4
Beilstein/REAXYS Number:
2059026
MDL number:

1 130,00 CZK


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biological source

synthetic (organic)

Quality Segment

assay

≥98%

form

powder

solubility

ethanol: soluble 10 mg/mL, clear, colorless to faintly yellow

functional group

ketone

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@@]12CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])C(C)=O

InChI

1S/C21H32O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h4,15-19,23H,5-12H2,1-3H3/t15-,16-,17+,18-,19-,20-,21+/m0/s1

InChI key

ORNBQBCIOKFOEO-QGVNFLHTSA-N

Gene Information

human ... SERPINA6(866)
rat ... Ar(24208)

Application

5-Pregnen-3β-ol-20-one is suitable for use:
  • as a substrate for 3β-HSD at a concentration of 1 μg/mL to study the time-dependent effect of reduced oxygen tension on 3β-hydroxysteroid dehydrogenase (3β-HSD) activity
  • as a progestin precursor to study the effects of splenic macrophages on progestin secretion of luteal cells
  • in the testicular interstitial cell culture medium at a concentration of 15mg/mL

Biochem/physiol Actions

Testosterone production in rats occurs in Leydig cells of the testis via the Δ4 pathway. Cholesterol is first converted to pregnenolone, then to progesterone, and finally to testosterone. Pregnenolone is the key neurosteroid synthesized in steroidogenic glands. It is also present as a sulfate ester that serves as an antagonist of GABAergic neurons by interacting with γ-aminobutyric acid (GABA) receptor.
One of a small number of "neurosteroids," steroids synthesized in the brain rather than peripheral sources. Decreased levels of these neurosteroids has been implicated in rodent cognitive decline with age, but studies in humans have been contradictory.

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700142PPHR2564P8129
description

≥98%

description

Avanti Research™ - A Croda Brand

description

Pharmaceutical Secondary Standard; Certified Reference Material

description

-

biological source

synthetic (organic)

biological source

-

biological source

-

biological source

synthetic (organic)

assay

≥98%

assay

>99% (TLC)

assay

-

assay

≥98% (TLC)

functional group

ketone

functional group

-

functional group

-

functional group

-

shipped in

ambient

shipped in

dry ice

shipped in

-

shipped in

ambient

solubility

ethanol: soluble 10 mg/mL, clear, colorless to faintly yellow

solubility

-

solubility

-

solubility

chloroform: 50 mg/mL, clear, colorless

form

powder

form

powder

form

solid

form

powder


Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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